Evidence map›Paper›PMID 31999935›Full record

ArticleBosnian journal of basic medical sciences2020

Concordance of PD-L1 expression and CD8+ TIL intensity between NSCLC and synchronous brain metastases.

Sebnem Batur, Onur Dulger, Sermin Durak, Perran Fulden Yumuk, Hale Basak Caglar, Emine Bozkurtlar, Suheyla Bozkurt, Ebru Tastekin, Irfan Cicin, Rengin Ahiskali and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Bosnian journal of basic medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Sebnem BaturDepartment of Pathology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Onur DulgerDepartment of Pathology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Sermin DurakDepartment of Pathology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Perran Fulden YumukDepartment of Internal Medicine, Division of Medical Oncology, Pendik Education and Research Hospital, School of Medicine, Marmara University, Istanbul, Turkey.
Hale Basak CaglarDepartment of Radiation Oncology, Medipol University, Istanbul, Turkey.
Emine BozkurtlarDepartment of Pathology, School of Medicine, Marmara University, Istanbul, Turkey.
Suheyla BozkurtDepartment of Pathology, School of Medicine, Marmara University, Istanbul, Turkey.
Ebru TastekinDepartment of Pathology, Medical Faculty, Trakya University, Edirne, Turkey.
Irfan CicinDepartment of Internal Medicine, Division of Medical Oncology, Trakya University, Edirne, Turkey.
Rengin AhiskaliDepartment of Pathology, School of Medicine, Marmara University, Istanbul, Turkey.
Rashad RzazadeDepartment of Radiation Oncology, Anatolia Health Center, Gebze, Turkey.
Asli CakirDepartment of Internal Medicine, Division of Medical Oncology, Medipol University, Istanbul, Turkey.
Buge OzDepartment of Pathology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Istanbul University-Cerrahpaşa · TRMarmara University · TRIstanbul Medipol University · TRTrakya University · TRTurkish Society of Hematology · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed death-ligand 1 (PD-L1) is suggested to be a predictive biomarker in non-small-cell lung carcinoma (NSCLC). However, the differential expression of PD-L1 in primary lung tumor vs. synchronous metastases, especially brain metastasis (BM), remains unclear. This study assessed the concordance of PD-L1 expression on tumor cells and tumor-infiltrating lymphocytes (TILs) and CD8+ TIL intensity between primary lung tumors and synchronous BMs from 24 NSCLC patients. PD-L1, CD3, and CD8 positivity was determined by immunohistochemistry (IHC). PD-L1 scoring was based on the proportion of tumor cells with membranous expression of PD-L1 and the cutoff values <1%, 1-49%, and ≥50%. CD3 and CD8 positivity in TILs was evaluated semi-quantitatively and the proportion of CD3+/CD8+ TILs was determined. PD-L1 expression on tumor cells and TILs was evaluated in relation to CD3+/CD8+ TIL proportions and the intensity of CD8+ TILs between the paired primary lung and BM tissues. In the primary lung tumors, PD-L1 positivity was observed in 25%, 37.5%, and 37.5% cases for the cutoff values <1%, 1-49%, and ≥50%, respectively. PD-L1 expression on tumor cells was strongly correlated between the paired primary lung and BM tissues, in all cutoff groups. However, PD-L1 expression on TILs and the proportion of CD3+/CD8+ TILs were not strongly correlated in all three groups between the paired primary lung tumors and BMs. The intensity of CD8+ TILs was concordant in only 54.16% of the paired primary lung tumors and BMs. This study showed a high concordance of PD-L1 expression in neoplastic cells between primary NSCLC and synchronous BMs.

Indexed as

AgedB7-H1 AntigenBrain NeoplasmsCarcinoma, Non-Small-Cell LungCD8-Positive T-LymphocytesFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasms, Multiple PrimaryTumor MicroenvironmentB7-H1 AntigenCD274 protein, human

Identifiers

PMID31999935
PMCPMC7416171
OpenAlexW2997018338

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.